Search
Search
About
Log in
Join
Experiences with
Blood ketone test
Posts
Communities
118,881 public posts
Filter results
Ketones inhibit PCa, in the lab of course, but still...
Just came across an article about this study from Duke researchers. Interesting possibility for dietary intervention? Researchers stress that it's not about the diet, but presence of ketones.
Just came across an article about this study from Duke researchers. Interesting possibility for dietary intervention? Researchers stress that it's not about the diet, but presence of ketones.
FRTHBST
in
Advanced Prostate Cancer
1 month ago
Prednisolone and diabetes / high bp worried sick about all the side effects
hi everyone I was diagnosed with PMR in February this year And despite being a diabetic with high bp was put on Prednisolone and alendronic acid - I was managing my diabetes with food prior to this but have now got out of control readings with ketones present in every reading except my blood fasting
hi everyone I was diagnosed with PMR in February this year And despite being a diabetic with high bp was put on Prednisolone and alendronic acid - I was managing my diabetes with food prior to this but have now got out of control readings with ketones present in every reading except my blood fasting
Pol53
in
PMRGCAuk
2 months ago
Hypochondria
Hypochondria, thy name is Kevin. My first bout with cancer was when I was 5 yrs old. I was just learning to read and was leafing through Life Magazine. I saw a poster-board titled, "The Seven Deadly Signs of Cancer." A few days prior I had noticed a lump near my nipple. When I read The Seven
Hypochondria, thy name is Kevin. My first bout with cancer was when I was 5 yrs old. I was just learning to read and was leafing through Life Magazine. I saw a poster-board titled, "The Seven Deadly Signs of Cancer." A few days prior I had noticed a lump near my nipple. When I read The Seven
kaypeeoh
in
Cure Parkinson's
10 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
PMR relapse?
I would be grateful for some advice! I was diagnosed with PMR end of 2022. I was put on 15 mg Prednisolone and started tapering around 2 months in. I stopped Pred December 23! Around 10 weeks ago started waking in early hours in bad pain chiefly in shoulders and hips but also shooting pains in limbs
I would be grateful for some advice! I was diagnosed with PMR end of 2022. I was put on 15 mg Prednisolone and started tapering around 2 months in. I stopped Pred December 23! Around 10 weeks ago started waking in early hours in bad pain chiefly in shoulders and hips but also shooting pains in limbs
mandian
in
PMRGCAuk
2 hours ago
Johns Hopkins adjusted clinical groups system score mean under nhs?
I see this on record Johns Hopkins adjusted clinical groups system score of ACG 5. What does it mean how does it impact me in any way.? I have started asking for blood tests and my GP has not been happy about it. Surgery has never been keen to blood tests though this seems to have popped up on record
I see this on record Johns Hopkins adjusted clinical groups system score of ACG 5. What does it mean how does it impact me in any way.? I have started asking for blood tests and my GP has not been happy about it. Surgery has never been keen to blood tests though this seems to have popped up on record
thyroidsymtoms
in
Thyroid UK
14 hours ago
Discharged by rheumy!
I went to my appointment yesterday, full of tales of woe about all my various health problems this year which caused a delay in my tapering. I'm on half a mg pred. He said my blood tests were all fine. I've had no recurrence of any GCA symptoms. My hip and shoulder stiffness (which is constant and not
I went to my appointment yesterday, full of tales of woe about all my various health problems this year which caused a delay in my tapering. I'm on half a mg pred. He said my blood tests were all fine. I've had no recurrence of any GCA symptoms. My hip and shoulder stiffness (which is constant and not
Broseley
in
PMRGCAuk
16 hours ago
Time between Afib trigger & episode
Hi all, I've very recently been diagnosed with Afib (thanks, Apple Watch for highlighting the problem I'd never heard of) and have been to the GP/hospital since February to get a proper diagnosis. So far all my results are showing normal (blood pressure, Echo, blood tests, that sort of thing). ECG did
Hi all, I've very recently been diagnosed with Afib (thanks, Apple Watch for highlighting the problem I'd never heard of) and have been to the GP/hospital since February to get a proper diagnosis. So far all my results are showing normal (blood pressure, Echo, blood tests, that sort of thing). ECG did
MrBinks
in
Atrial Fibrillation Support
17 hours ago
New diagnose - GMG
Was diagnosed with FM January 2020, never got a follow-up because of COVID-19, just increasing the medication from GP. Previous winter 22-23 was BAD!!! Didn't leave the house, almost all the winter in bed. Horrible pain, itching that hurts, shaking, and on and on...Till began to slur words, chock on
Was diagnosed with FM January 2020, never got a follow-up because of COVID-19, just increasing the medication from GP. Previous winter 22-23 was BAD!!! Didn't leave the house, almost all the winter in bed. Horrible pain, itching that hurts, shaking, and on and on...Till began to slur words, chock on
Polly-S
in
Fibromyalgia Action UK
18 hours ago
My question is about the best way of getting a diagnosis of sarcoidosis or of discounting it?
I was diagnosed recently with Raynauds disease which can get quie painful, but is manageable. I have GORD and a small hiatus hernia. However I do get abdominal pain and have asthma exacerbated by allergies. I have just had a CT scan and was told the pain is probably musco-skeletal, plus I have an atryphed
I was diagnosed recently with Raynauds disease which can get quie painful, but is manageable. I have GORD and a small hiatus hernia. However I do get abdominal pain and have asthma exacerbated by allergies. I have just had a CT scan and was told the pain is probably musco-skeletal, plus I have an atryphed
strongmouse
in
Scleroderma & Raynaud's UK (SRUK)
1 day ago
Active B12 29 (37.5-150)
These are my student daughter's results. She is at uni in Edinburgh and struggling to find g.p. practice to take her on. She has an iron panel coming too but sample haemolised so have to redo it. These are first blood tests and she is not taking any supplements. Please advise on thoughts and next
These are my student daughter's results. She is at uni in Edinburgh and struggling to find g.p. practice to take her on. She has an iron panel coming too but sample haemolised so have to redo it. These are first blood tests and she is not taking any supplements. Please advise on thoughts and next
AKatieD
in
Pernicious Anaemia Society
1 day ago
On ending
Just over 2 months ago I had 2value.replacements mechanical op went very well unfortunately my after care didn't go all that well .Iam having to go to doctors 2 times a week.for blood tests to get warfine dose right and this week alone 2 hospital appointments.which is far way don't have car and patent
Just over 2 months ago I had 2value.replacements mechanical op went very well unfortunately my after care didn't go all that well .Iam having to go to doctors 2 times a week.for blood tests to get warfine dose right and this week alone 2 hospital appointments.which is far way don't have car and patent
Craig53
in
British Heart Foundation
1 day ago
PMR since July 2018 and down to 1mg. Enter GCA
My Bio is pretty well up to date, until a week ago. Quick summary of things is: I'm ok, vision ok, diagnosed with GCA, and I've gone from 1mg (nearly done...or so I thought) to 60mg. Now on my third day of 60mg and waiting on new bloods I did today and a call from the consultant tomorrow to discuss
My Bio is pretty well up to date, until a week ago. Quick summary of things is: I'm ok, vision ok, diagnosed with GCA, and I've gone from 1mg (nearly done...or so I thought) to 60mg. Now on my third day of 60mg and waiting on new bloods I did today and a call from the consultant tomorrow to discuss
pata63
in
PMRGCAuk
2 days ago
Confusing Lab Test Results
I had a recent PMR flare that necessitated my temporarily going up from the 5mg I had tapered down to to a much higher dose. 20mg for 2 weeks, followed by 15mg for one week and then a drop to 10mg, where I have stayed for almost a month before I resume DL’s slow 5 week taper. Fortunately, my increased
I had a recent PMR flare that necessitated my temporarily going up from the 5mg I had tapered down to to a much higher dose. 20mg for 2 weeks, followed by 15mg for one week and then a drop to 10mg, where I have stayed for almost a month before I resume DL’s slow 5 week taper. Fortunately, my increased
Donna5658
in
PMRGCAuk
2 days ago
Interpreting blood tests
I've been on ADT for 4 months in preparation for RT and then HDR BT. I have localised G8 with an initial PSA of 8.1 Prior to commencing ADT, my PSA inexplicably dropped to 4.94 but then rose to 5.37 within 2 months. Anyway, here are my test results before starting ADT; These are Aussie measurements
I've been on ADT for 4 months in preparation for RT and then HDR BT. I have localised G8 with an initial PSA of 8.1 Prior to commencing ADT, my PSA inexplicably dropped to 4.94 but then rose to 5.37 within 2 months. Anyway, here are my test results before starting ADT; These are Aussie measurements
Mike58
in
Advanced Prostate Cancer
2 days ago
Silent Reflux? Is yours scary?
Initially I could just be having a drink of water from a bottle and suddenly spray the water straight back out of my mouth. No warning. No previous symptoms either. After a scan and blood tests that were fine, in a week it stopped. 3 months down the track, the left hand side of tongue and under tongue
Initially I could just be having a drink of water from a bottle and suddenly spray the water straight back out of my mouth. No warning. No previous symptoms either. After a scan and blood tests that were fine, in a week it stopped. 3 months down the track, the left hand side of tongue and under tongue
MeeMawMea
in
Acid Reflux Support
2 days ago
B vits
I think I need to start taking b vits again as feeling very foggy brained, apathetic etc. I stopped as ineggus b complex seemed to be exacerbating a pain under my right rib. I stopped taking them and the pain ceased. I tried one tablet again last week and the pain returned. I’ve had a chest x ray and
I think I need to start taking b vits again as feeling very foggy brained, apathetic etc. I stopped as ineggus b complex seemed to be exacerbating a pain under my right rib. I stopped taking them and the pain ceased. I tried one tablet again last week and the pain returned. I’ve had a chest x ray and
Fizzwhizz
in
Thyroid UK
2 days ago
experiences with seasonal changes?
If you have taken thyroid hormone replacement for some time and your levels are pretty much settled please can you share your experiences with seasonal changes? Do you find you need to reduce/increase your doses seasonally? What signs apart from blood test results indicate this if so?
If you have taken thyroid hormone replacement for some time and your levels are pretty much settled please can you share your experiences with seasonal changes? Do you find you need to reduce/increase your doses seasonally? What signs apart from blood test results indicate this if so?
Regenallotment
in
Thyroid UK
2 days ago
Red Cell Distribution Width
Hi…my blood tests have been showing ‘normal’ fr Crp Esr …everything except a consistently high Red cell distribution width above 18 I have been diagnosed with GCA but could this mean more likely Vasculitis am worried
Hi…my blood tests have been showing ‘normal’ fr Crp Esr …everything except a consistently high Red cell distribution width above 18 I have been diagnosed with GCA but could this mean more likely Vasculitis am worried
Havanahula
in
PMRGCAuk
2 days ago
Positive mitochondrial antibodies m2 but normal liver enzymes
Hi members, just after a bit of advice please. I have hashimoto's and due to blood tests which were requested by my endocrinologist, positive mitochondrial antibodies m2 were found which he says could mean it is primary biliary cholangitis. I went for an ultrasound and I am due to have a consultation
Hi members, just after a bit of advice please. I have hashimoto's and due to blood tests which were requested by my endocrinologist, positive mitochondrial antibodies m2 were found which he says could mean it is primary biliary cholangitis. I went for an ultrasound and I am due to have a consultation
Ladysmith53
in
PBC Foundation
2 days ago
Long, rambing, mostly incoherent post (re B12)
Okay, so a few months ago, I was injecting once a week, then twice a week and so on working my way towards every day...I was injecting EOD, when I got a form from the social welfare demanding to know why I'd not gotten a job etc (they do this to me every 6 months or so). Part of the form asked (indirectly
Okay, so a few months ago, I was injecting once a week, then twice a week and so on working my way towards every day...I was injecting EOD, when I got a form from the social welfare demanding to know why I'd not gotten a job etc (they do this to me every 6 months or so). Part of the form asked (indirectly
Saoirse2016
in
Pernicious Anaemia Society
2 days ago
1
2
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Thyroid UK
66942 results
Fertility Network UK
5788 results
Pernicious Anaemia Society
4815 results
View top 10 communities
Sort by
Most Relevant
Newest